A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9536n152



Internal ID22825239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34643734..34644330hg38UCSC Ensembl
chr9:34643731..34644327hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3226808, nsv3211425
SamplesHG00512, HG00514
Known Genes
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9536n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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